Haku
Viitteet 1-6 / 6
- Lajitteluvaihtoehdot:
- Relevanssi
- Nimeke (Ö-A)
- Nimeke (A-Ö)
- Julkaisuaika (nouseva)
- Julkaisuaika (laskeva)
- Syöttöaika (nouseva)
- Syöttöaika (laskevat)
- Tuloksia per sivu:
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Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Kathiresan S; Voight B; Purcell S; Musunuru K; Ardissino D; Mannucci PM; Anand S; Engert JC; Samani NJ; Schunkert H; Erdmann J; Reilly MP; Rader DJ; Morgan T; Spertus JA; Stoll M; Girelli D; McKeown PP; Patterson CC; Siscovick DS; ODonnell CJ; Elosua R; Peltonen L; Salomaa V; Myocardial Infarction Genetics Consortium Group (2009)
Common variants at 30 loci contribute to polygenic dyslipidemia
Kathiresan S; Willer CJ; Peloso GM; Demissie S; Musunuru K; Schadt EE; Kaplan L; Bennett D; Li Y; Tanaka T; Voight BF; Bonnycastle LL; Jackson AU; Crawford G; Surti A; Guiducci C; Burtt NP; Parish S; Clarke R; Zelenika D; Kubalanza KA; Morken MA; Scott LJ; Stringham HM; Galan P; Swift AJ; Kuusisto J; Bergman RN; Sundvall J; Laakso M; Ferrucci L; Scheet P; Sanna S; Uda M; Yang Q; Lunetta KL; Dupuis J; de Bakker PIW; Chambers JC; Kooner JS; Hercberg S; Meneton P; Lakatta EG; Scuteri A; Schlessinger D; Tuomilehto J; Collins FS; Groop L; Altshuler D; Collins R; Lathrop GM; Melander O; Salomaa V; Peltonen L; Orho-Melander M; Ordovas JM; Boehnke M; Abecasis GR; Mohlke KL; Cupples LA (2009)
Genome-wide association study identifies eight loci associated with blood pressure
Newton-Cheh C; Johnson T; Gateva V; Tobin MD; Bochud M; Coin L; Najjar SS; Zhao JH; Heath SC; Eyheramendy S; Papadakis K; Voight BF; Scott LJ; Zhang F; Farrall M; Tanaka T; Wallace C; Chambers JC; Khaw KT; Nilsson P; van der Harst P; Polidoro S; Grobbee DE; Onland-Moret NC; Bots ML, Wain LV; Elliott KS; Teumer A; Luan J; Lucas G; Kuusisto J; Burton PR; Hadley D; McArdle WL; Brown M; Dominiczak A; Newhouse SJ; Samani NJ; Webster J; Zeggini E; Beckmann JS; Bergmann S; Lim N; Song K; Vollenweider P; Waeber G; Waterworth DM; Yuan X; Groop L; Orho-Melander M; Allione A; Di Gregorio A; Guarrera S; Panico S; Ricceri F; Romanazzi V; Sacerdote C; Vineis P; Barroso I; Sandhu MS; Luben RN; Crawford GJ; Jousilahti P; Perola M; Boehnke M; Bonnycastle LL; Collins FS; Jackson AU; Mohlke KL; Stringham HM; Valle TT; Willer CJ; Bergman RN; Morken MA; Doring A; Gieger C; Illig T; Meitinger T; Org E; Pfeufer A; Wichmann HE; Kathiresan S; Marrugat J; Schwartz SM; Siscovick DS; Subirana I; Freimer NB; Hartikainen AL; McCarthy MI; Peltonen L; Pouta A; de Jong PE; Snieder H; van Gilst WH; Clarke R; Goel A; Hamsten A; Peden JF; Seedorf U; Syvänen AC; Tognoni G; Lakatta EG; Sanna S; Scheet P; Schlessinger D; Scuteri A; Dorr M; Ernst F; Felix SB; Homuth G; Lorbeer R; Reffelmann T; Rettig R; Volker U; Galan P; Gut IG; Hercberg S; Lathrop GM; Zelenika D; Deloukas P,; Soranzo N; Williams FM; Zhai G; Salomaa V; Laakso M; Elosua R (2009)
Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure
Newton-Cheh C; Larson MG; Vasan RS; Levy D; Bloch KD; Surti A; Guiducci C; Kathiresan S; Benjamin EJ; Struck J; Morgenthaler NG; Bergmann A; Blankenberg S; Kee F; Nilsson P; Yin X; Peltonen L; Vartiainen E; Salomaa V; Hirschhorn JN; Melander O; Wang TJ (2009)
Genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Soranzo N; Spector TD; Mangino M; Kühnel B; Rendon A; Teumer A; Willenborg C; Wright B; Chen L; Li M; Salo P; Voight BF; Burns P; Laskowski RA; Xue Y; Menzel S; Altshuler D; Bradley JR; Bumpstead S; Burnett MS; Devaney J; Döring A; Elosua R; Epstein SE; Erber W; Falchi M; Garner SF; Ghori MJ; Goodall AH; Gwilliam R; Hakonarson HH; Hall AS; Hammond N; Hengstenberg C; Illig T; König IR; Knouff CW; McPherson R; Melander O; Mooser V; Nauck M; Nieminen MS; Peltonen L; Potter SC; Prokisch H; Rader DJ; Rice CM; Roberts R; Salomaa V; Sambrook J; Schreiber S; Schunkert H; Schwartz SM; Serbanovic-Canic J; Sinisalo J; Siscovick DS; Stark K; Surakka I; Stephens J; Thompson JR; Völker U; Völzke H; Watkins NA; Wells GA; Wichmann HE; Van Heel DA; Tyler-Smith C; Thein SL; Kathiresan S; Perola M; Reilly MP; Stewart AF; Erdmann J; Samani NJ; Meisinger C; Greinacher A; Deloukas P; Ouwehand WH; Gieger C (2009)
New susceptibility locus for coronary artery disease on chromosome 3q22.3
Erdmann J; Grosshennig A; Braund PS; König IR; Hengstenberg C; Hall AS; Linsel-Nitschke P; Kathiresan S; Wright B; Trégouët DA; Cambien F; Bruse P; Aherrahrou Z; Wagner AK; Stark K; Schwartz SM; Salomaa V; Elosua R; Melander O; Voight BF; Peltonen L; Siscovick DS; Altshuler D; Merlini PA; Peyvandi F; Bernardinelli L; Ardissino D; Schillert A; Blankenberg S; Zeller T; Wild P; Schwarz DF; Tiret L; Perret C; Schreiber S; El Mokhtari NE; Schäfer A; März W; Renner W; Bugert P; Klüter H; Schrezenmeir J; Rubin D; Ball SG; Balmforth AJ; Wichmann HE; Meitinger T; Fischer M; Meisinger C; Baumert J; Peters A; Ouwehand WH;; Italian Atherosclerosis, Thrombosis, and Vascular Biology Wo; Myocardial Infarction Genetics Consortium; Wellcome Trust Case Control Consortium; Cardiogenics Consortium; Deloukas P; Thompson JR; Ziegler A; Samani NJ; Schunkert H (2009)